A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17120046



Internal ID21496376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:173583715..173583766hg38UCSC Ensembl
chr4:174504866..174504917hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5576537
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17120046
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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